rs786205613
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs786205613(-;-) |
Make rs786205613(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 84203048 |
Gene | CDHR1 |
is a | snp |
is | mentioned by |
dbSNP | rs786205613 |
dbSNP (classic) | rs786205613 |
ClinGen | rs786205613 |
ebi | rs786205613 |
HLI | rs786205613 |
Exac | rs786205613 |
Gnomad | rs786205613 |
Varsome | rs786205613 |
LitVar | rs786205613 |
Map | rs786205613 |
PheGenI | rs786205613 |
Biobank | rs786205613 |
1000 genomes | rs786205613 |
hgdp | rs786205613 |
ensembl | rs786205613 |
geneview | rs786205613 |
scholar | rs786205613 |
rs786205613 | |
pharmgkb | rs786205613 |
gwascentral | rs786205613 |
openSNP | rs786205613 |
23andMe | rs786205613 |
SNPshot | rs786205613 |
SNPdbe | rs786205613 |
MSV3d | rs786205613 |
GWAS Ctlg | rs786205613 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205613(-;-) |
Alt | rs786205613(-;-) |
Reference | Rs786205613(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CDHR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.85962804delG |
CLNSRC | |
CLNACC | RCV000171458.1, |